Maffucci’s syndrome is a congenital, non-hereditary mesodermal dysplasia manifested by multiple enchondromas and hemangiomas.
1. Carleton A, Elkington J, Greenfield JG, et a l . M a f f u c c i ‘ s s y n d r o m e (dyschondroplasia with hemangiomata).Q J Med 1942;35:203-28
4. Gao H,WangB,ZhangX,LiuF,Lu Y. Maffucci syndrome with unilateral limb: a case report and review of literature. Chin J Cancer Res 2103;25(2):245-258.
2. McDermott AL, Dutt SN, Chavda SV, et al. Maffucci’s syndrome: clinical and radiological features of a rare condition. J Laryngol Otol, 2001;115:845-7.
3. Lewis RJ, Ketcham AS. Maffucci’s syndrome:functional and neoplastic significance—case report and review of the literature. J Bone Joint Surg Am 1973; 55:1465–1479.
5. Mainzer F, Minagi H, Steinbach HL. The variable manifestations of multiple enchondromatosis. Radiology 1971; 99:377–388.
6. Unroe BJ, Kissel CG, Rosenberg JC. Maffucci’s syndrome. Review of the literature and case report. J Am Pediatr Med Assoc1992;82:532-6.
7. Schwarzt HS, Zimmerman NB, Simon MA, et al. The malignant potential of enchondromatosis. J Bone Joint Surg 1987;69A:269-74.
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